A Randomized, Double-Blind, Placebo-Controlled Trial of Citicoline in Patients with Alcohol Use Disorder

被引:12
作者
Brown, E. Sherwood [1 ]
Van Enkevort, Erin [1 ]
Kulikova, Alexandra [1 ]
Escalante, Chastity [1 ]
Nakamura, Alyson [1 ]
Ivleva, Elena I. [1 ]
Holmes, Traci [1 ]
机构
[1] Univ Texas Southwestern Med Ctr Dallas, Dept Psychiat, Dallas, TX 75390 USA
来源
ALCOHOL-CLINICAL AND EXPERIMENTAL RESEARCH | 2019年 / 43卷 / 02期
关键词
Citicoline; Alcohol Use Disorder; Clinical Trial; Cognition; CDP-CHOLINE; DEPENDENCE; TOPIRAMATE; ACAMPROSATE; EFFICACY; BIPOLAR; METAANALYSIS; DISULFIRAM; MECHANISMS; NALTREXONE;
D O I
10.1111/acer.13928
中图分类号
R194 [卫生标准、卫生检查、医药管理];
学科分类号
摘要
Background Alcohol use disorder is a major societal and individual burden that exacerbates health outcomes, decreases quality of life, and negatively affects U.S. healthcare spending. Although pharmacological treatments are available for alcohol use disorder, many of them are limited by small effect sizes and used infrequently. Citicoline is a widely available over-the-counter supplement with a favorable side effect profile. It acts through cholinergic pathways and phospholipid metabolism. The current report examines the effect of oral citicoline on alcohol use, craving, depressive symptoms, and cognitive outcomes in individuals with alcohol use disorder. Methods A 12-week, randomized, double-blind, parallel-group, placebo-controlled, pilot study of citicoline (titrated to 2,000 mg/d) in 62 adults (age 18 to 75) with alcohol use disorder was conducted. Alcohol use, such as number of drinking days, amount used, and number of heavy drinking days, was assessed using the Timeline Followback method and liver enzymes, while alcohol craving was measured using the Penn Alcohol Craving Scale. A neurocognitive battery (e.g., Rey Auditory Verbal Learning Test) and depressive symptoms scale (e.g., Inventory of Depressive Symptomatology Self-Report) scores were also collected. Data were analyzed using a random regression analysis. Results The primary outcome analysis was conducted in the intent-to-treat sample and consisted of 55 participants (78.2% men and 21.8% women, mean age of 46.47 +/- 9.15 years). In the assessment period, the drinking days, on average, represented 77% of the assessed days. Significant between-group differences were not observed on alcohol use, craving, and cognitive or depressive symptom measures. Citicoline was well tolerated. Conclusions This proof-of-concept study observed that citicoline was well tolerated, but was not associated with a reduction in alcohol use or other outcomes, as compared to placebo. The favorable effects reported with citicoline for cocaine use, cognitive disorders, and other conditions do not appear to extend to alcohol use disorder.
引用
收藏
页码:317 / 323
页数:7
相关论文
共 45 条
[1]   Citicoline mechanisms and clinical efficacy in cerebral ischemia [J].
Adibhatla, RM ;
Hatcher, JF .
JOURNAL OF NEUROSCIENCE RESEARCH, 2002, 70 (02) :133-139
[2]  
Alkan T., 2001, Archives of Physiology and Biochemistry, V109, P161, DOI 10.1076/apab.109.2.161.4273
[3]  
[Anonymous], 1995, PSIQUIAT BIOL
[4]  
Baddeley A.D., 1986, WORKING MEMORY
[5]   A randomized, placebo-controlled trial of citicoline add-on therapy in outpatients with bipolar disorder and cocaine dependence [J].
Brown, E. Sherwood ;
Gorman, April R. ;
Hynan, Linda S. .
JOURNAL OF CLINICAL PSYCHOPHARMACOLOGY, 2007, 27 (05) :498-502
[6]   A Randomized, Double-Blind, Placebo-Controlled Trial of Citicoline for Cocaine Dependence in Bipolar I Disorder [J].
Brown, E. Sherwood ;
Todd, Jackie Peterson ;
Hu, Lisa T. ;
Schmitz, Joy M. ;
Carmody, Thomas J. ;
Nakamura, Alyson ;
Sunderajan, Prabha ;
Rush, A. John ;
Adinoff, Bryon ;
Bret, Mary Ellen ;
Holmes, Traci ;
Lo, Alexander .
AMERICAN JOURNAL OF PSYCHIATRY, 2015, 172 (10) :1014-1021
[7]   A randomized, double-blind, placebo-controlled trial of citicoline for bipolar and unipolar depression and methamphetamine dependence [J].
Brown, E. Sherwood ;
Gabrielson, Barry .
JOURNAL OF AFFECTIVE DISORDERS, 2012, 143 (1-3) :257-260
[8]   New steps for treating alcohol use disorder [J].
Campbell, Erin J. ;
Lawrence, Andrew J. ;
Perry, Christina J. .
PSYCHOPHARMACOLOGY, 2018, 235 (06) :1759-1773
[9]   Comparative study of the effects of short- and long-term ethanol treatment and alcohol withdrawal on phospholipid biosynthesis in rat hepatocytes [J].
Carrasco, MP ;
Jiménez-López, JM ;
Segovia, JL ;
Marco, C .
COMPARATIVE BIOCHEMISTRY AND PHYSIOLOGY B-BIOCHEMISTRY & MOLECULAR BIOLOGY, 2002, 131 (03) :491-497
[10]  
Carter MJ, 2014, THER RECREAT J, V48, P275